Device recall
Z-1358-2018: Doyen-Collin Mouth Gag 120MM/ General Instruments
FDA device recall · Class III · Aesculap Implant Systems LLC
Key facts
| Recall number (Z-number) | Z-1358-2018 |
|---|---|
| Recall event | 79656 |
| Product | Doyen-Collin Mouth Gag 120MM/ General Instruments |
| Product code | KBN |
| Recalling firm | Aesculap Implant Systems LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 30, 2020 |
| FEI number | 2916714 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database